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Biodegradable triblock copolymer microspheres for drug delivery based on thermosensitive property of triblock copolymer.

机译:基于三嵌段共聚物的热敏性质的可生物降解的三嵌段共聚物微球用于药物递送。

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摘要

Extensive research has recently been focused on injectable polymeric drug delivery system for the delivery of bioactive agents such as anticancer agents, proteins, or DNA in the form of drug-loaded particulate systems (i.e., microspheres and nanoparticles) for the last decade.; Conventional protein-loaded microsphere preparation involves use of water-immiscible organic solvent such as methylene chloride under harsh condition and the resultant microsphere typically exhibits initial burst effect followed by incomplete release of protein drug. An experiment was designed to monitor insulin aggregation induced by water/methylene chloride interface by a turbidimetric method. Insulin at the interface quickly underwent aggregation. This paved the way for a novel approach to prepare biodegradable microspheres without using organic solvent by utilizing unique aqueous sol-gel transition property of triblock copolymer poly(lactic-co-glycolic acid) (PLGA)-PEG-PLGA.; A comparative study was carried out using microspheres of the same polymer and drug but prepared by different methods: Msp A (water-based microsphere) and Msp B (w/o/w). Insulin release was carried out in vitro and Msp A showed continuous release over 2 weeks while Msp B exhibited an initial burst effect followed by no release. Circular dichroism (CD) spectroscopy of released insulin demonstrated that insulin from Msp A maintained secondary structure integrity while that from Msp B did not. Confocal microcopy of FITC-labeled insulin showed that fluorescence was homogeneous in Msp A but not homogeneous in Msp B. In an in vivo study using streptozotocin-induced diabetic rats, Msp B exhibited an initial burst release as shown by hypoglycemic shock while Msp A showed less burst and prolonged release for 10 days.; The versatility of this triblock copolymer led to the design of an aqueous-based nanoparticle carrier for paclitaxel. Drug-loaded nanoparticle demonstrated control of cultured vascular smooth muscle cell proliferation for potential treatment of restenosis.; The unique property of thermosensitive, biodegradable triblock copolymer made it possible to design novel methods of preparing organic solvent-free particulate systems for the delivery of protein and water-insoluble drug.
机译:最近,广泛的研究集中在可注射的聚合物药物输送系统上,以在过去十年中以载药颗粒系统(即微球和纳米颗粒)的形式输送生物活性剂,例如抗癌剂,蛋白质或DNA。常规的载有蛋白质的微球制备涉及在恶劣条件下使用与水不混溶的有机溶剂,例如二氯甲烷,并且所得的微球通常表现出最初的爆发效应,随后是蛋白质药物的不完全释放。设计了一个通过比浊法监测水/二氯甲烷界面诱导的胰岛素聚集的实验。界面处的胰岛素迅速聚集。这通过利用三嵌段共聚物聚(乳酸-乙醇酸)(PEGA)-PEG-PLGA的独特的水溶胶-凝胶转变性质,为无需使用有机溶剂制备可生物降解的微球的新方法铺平了道路。使用相同聚合物和药物但通过不同方法制备的微球进行了比较研究:Msp A(水基微球)和Msp B(w / o / w)。胰岛素的释放在体外进行,其Msp A在2周内连续释放,而Msp B则表现出最初的爆发效应,随后没有释放。释放的胰岛素的圆二色性(CD)光谱表明,来自Msp A的胰岛素保持二级结构完整性,而来自Msp B的胰岛素则没有。 FITC标记的胰岛素的共聚焦显微镜显示,Msp A中的荧光是均匀的,而Msp B中的荧光却不是均匀的。在一项使用链脲佐菌素诱导的糖尿病大鼠的 in vivo 研究中,Msp B表现出最初的爆发释放。低血糖休克,而Msp A的爆裂较少,释放时间延长了10天。这种三嵌段共聚物的多功能性导致了紫杉醇的水基纳米颗粒载体的设计。载药纳米颗粒显示出对培养的血管平滑肌细胞增殖的控制,可用于再狭窄的潜在治疗。热敏性,可生物降解的三嵌段共聚物的独特性能使得设计新颖的方法可以制备无有机溶剂的微粒体系,以输送蛋白质和水不溶性药物。

著录项

  • 作者

    Kwon, Young Min.;

  • 作者单位

    The University of Utah.;

  • 授予单位 The University of Utah.;
  • 学科 Health Sciences Pharmacy.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 151 p.
  • 总页数 151
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药剂学;
  • 关键词

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